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49S-Sulfo-Cysteine is an Endogenous Amino Acid in Neonatal Rat Brain but an Unlikely Mediator of Cysteine Neurotoxicity, Neurochemical Research Defective molybdopterin biosynthesis: clinical heterogeneity associated with molybdenum cofactor deficiency, Journal of Inherited Metabolic Disease Infantile isolated sulphite oxidase deficiency: Report of a case with negative sulphite test and normal sulphate excretion, European Journal of Pediatrics Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase, Journal of Inherited Metabolic Disease The effect of molybdenum cofactor deficiency on the purine pattern of cerebrospinal fluid, Journal of Inherited Metabolic Disease Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?, Journal of Inherited Metabolic Disease An unusual genetic variant in the MOCS1 gene leads to complete missplicing of an alternatively spliced exon in a patient with molybdenum cofactor deficiency, Journal of Inherited Metabolic Disease Molybdenum Cofactor Disorders, Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases